Amneal
Pharmaceuticals - Walk in Interview on 29th September, 2019 (Sunday) for
Manufacturing (OSD & Injectable)
Openings: 100
Openings: 100
We are looking for
competent, dynamic and motivated candidates for suitable positions for
Injectable & OSD (oral solid dosage) unit for our Ahmedabad SEZ Matoda
Plant.
We are Amneal and We make healthy possible.
Date: 29th September, 2019 (Sunday)
Timing: 9:00 AM to 12:00 PM
Venue:Amneal Pharmaceuticals Pvt. Ltd.
Plot No 15,16,17 Pharmez
Village: Matoda
Sarkhej Bavla Road, Abad
Please find the Job details below :
1.Manufacuturing (Tablet/Capsules)
Designation: Officer/Sr. Officer/Executive/Operators
Qualification: B.Pharm/ITI
Total experience: 01 to 05 years
Desired Profile :
1. Candidate should have experience in Solid Oral Granulation, Compression, Coating, Packing, Capsule filling, bulk packing etc.
2. The candidate with good communication and inter-personal skills, computer knowledge and exposure to cGMP / GLP, knowledge and understanding of Regulatory Requirement is essential.
We are Amneal and We make healthy possible.
Date: 29th September, 2019 (Sunday)
Timing: 9:00 AM to 12:00 PM
Venue:Amneal Pharmaceuticals Pvt. Ltd.
Plot No 15,16,17 Pharmez
Village: Matoda
Sarkhej Bavla Road, Abad
Please find the Job details below :
1.Manufacuturing (Tablet/Capsules)
Designation: Officer/Sr. Officer/Executive/Operators
Qualification: B.Pharm/ITI
Total experience: 01 to 05 years
Desired Profile :
1. Candidate should have experience in Solid Oral Granulation, Compression, Coating, Packing, Capsule filling, bulk packing etc.
2. The candidate with good communication and inter-personal skills, computer knowledge and exposure to cGMP / GLP, knowledge and understanding of Regulatory Requirement is essential.
3. Please
do not apply who are having API background
2.Sterile Manufacturing ( Injectable unit /Parenteral Unit)
Designation: Officer /Sr. Officer/Operators
Qualification: B.Pharm/M.sc/ITI/Diploma
Total Experience: 02 to 05 years
Desired Profile :
- To observe & follow all rules and regulations of the production department.
- Must be from Parenteral background
- To be aware and responsible for achieving quality objective and fulfilling the requirements of the quality of the companys service by means of applicable quality procedures.
- Sound technical knowledge of Aseptic area and controlled are related activities.
- Technical exposure and expertise on vial filling, sealing, Autoclave, Lyophilizer, PFS filling, cartridge filling machine.
- Knowledge of Regulatory guidelines and exposure of USFDA audits.
- Knowledge of Eye drop filling machine and related batch mfg. process.
- Knowledge of Quality Management System (QMS) i.e. change control, Deviation, CAPA, and documentation in manufacturing area of injectable.
- Expertise in batch manufacturing and preparation related activities.
- Knowledge of equipment validation and qualifications in injectable.
- The candidate with good communication and inter personal skills, computer knowledge and exposure to cGMP/GLP Knowledge and understanding of regulatory requirement is essential.
Note : Candidate should have 01 to 05 years of relevant experience in USFDA regulatory approved pharmaceuticals (Preferred 21 CFR compliance) organisation.
2.Sterile Manufacturing ( Injectable unit /Parenteral Unit)
Designation: Officer /Sr. Officer/Operators
Qualification: B.Pharm/M.sc/ITI/Diploma
Total Experience: 02 to 05 years
Desired Profile :
- To observe & follow all rules and regulations of the production department.
- Must be from Parenteral background
- To be aware and responsible for achieving quality objective and fulfilling the requirements of the quality of the companys service by means of applicable quality procedures.
- Sound technical knowledge of Aseptic area and controlled are related activities.
- Technical exposure and expertise on vial filling, sealing, Autoclave, Lyophilizer, PFS filling, cartridge filling machine.
- Knowledge of Regulatory guidelines and exposure of USFDA audits.
- Knowledge of Eye drop filling machine and related batch mfg. process.
- Knowledge of Quality Management System (QMS) i.e. change control, Deviation, CAPA, and documentation in manufacturing area of injectable.
- Expertise in batch manufacturing and preparation related activities.
- Knowledge of equipment validation and qualifications in injectable.
- The candidate with good communication and inter personal skills, computer knowledge and exposure to cGMP/GLP Knowledge and understanding of regulatory requirement is essential.
Note : Candidate should have 01 to 05 years of relevant experience in USFDA regulatory approved pharmaceuticals (Preferred 21 CFR compliance) organisation.
You may walk in
for interview with current CV along with CTC proof Appointment letter,
Increment letter & last 3 months salary slip & Bank statement, Aadhar
& PAN card and 2 passport size photograph.
If you are unable to attend interview you can share cv on chandanid@amnealindia.com , neha.modi@amnealindia.com , kishan.soni@amnealindia.com
With Regards
TEAM - HR
If you are unable to attend interview you can share cv on chandanid@amnealindia.com , neha.modi@amnealindia.com , kishan.soni@amnealindia.com
With Regards
TEAM - HR
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